Judith P. Willner
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 12
- Genetic Syndromes and Imprinting 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Congenital heart defects research 3
- Co-authors
- Robert J. Desnick (8 shared papers)Blanche P. Alter (2 shared papers)June A. Peters (2 shared papers)Sharon A. Savage (2 shared papers)Stephen J. Chanock (2 shared papers)Babette B. Weksler (2 shared papers)Peter M. Lansdorp (2 shared papers)Gabriela M. Baerlocher (2 shared papers)
- Journals
- Prenatal Diagnosis (4 papers)Pediatric Research (2 papers)Neurology (2 papers)Blood (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- United StatesSwitzerlandCanada
In The Last Decade
Judith P. Willner
33 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 83
- Clinical Biochemistry 116
- Genetics 457
- Physiology 287
- Sensory Systems 55
- Pediatrics, Perinatology and Child Health 158
Countries citing papers authored by Judith P. Willner
This map shows the geographic impact of Judith P. Willner's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Judith P. Willner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judith P. Willner more than expected).
Fields of papers citing papers by Judith P. Willner
This network shows the impact of papers produced by Judith P. Willner. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Judith P. Willner. The network helps show where Judith P. Willner may publish in the future.
Co-authors
The 25 scholars most cited alongside Judith P. Willner, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 252 | |
| 2 | 2013 | 239 | |
| 3 | 1994 | 99 | |
| 4 | 1997 | 83 | |
| 5 | 2003 | 72 | |
| 6 | 2002 | 67 | |
| 7 | 1981 | 62 | |
| 8 | 1998 | 58 | |
| 9 | Genetic testing: a physician's perspective. | 2000 | 44 |
| 10 | 1978 | 35 | |
| 11 | 2004 | 29 | |
| 12 | 2010 | 25 | |
| 13 | 1978 | 19 | |
| 14 | 1999 | 19 | |
| 15 | 1997 | 13 | |
| 16 | 1977 | 12 | |
| 17 | 1993 | 11 | |
| 18 | 2010 | 11 | |
| 19 | 2000 | 11 | |
| 20 | 1997 | 9 |
About Judith P. Willner
Judith P. Willner is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Physiology and Surgery, having authored 33 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers), Genetic Syndromes and Imprinting (4 papers), Metabolism and Genetic Disorders (3 papers), Congenital heart defects research (3 papers), Chromosomal and Genetic Variations (3 papers), Genetic Neurodegenerative Diseases (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Clinical Biochemistry (116 citations), Genetics (457 citations), Physiology (287 citations), Sensory Systems (55 citations) and Pediatrics, Perinatology and Child Health (158 citations). Judith P. Willner has collaborated with scholars based in United States, Switzerland and Canada. Frequent co-authors include Robert J. Desnick, Blanche P. Alter, June A. Peters, Sharon A. Savage, Stephen J. Chanock, Babette B. Weksler, Peter M. Lansdorp, Gabriela M. Baerlocher, Neelam Giri and Bruce D. Gelb. Their work appears in journals such as Prenatal Diagnosis, Pediatric Research, Neurology, Blood and The American Journal of Human Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.